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- W4236501171 abstract "DNA-encoded libraries of small molecules are being explored extensively for the identification of binders in early drug-discovery efforts. Combinatorial syntheses of such libraries require water- and DNA-compatible reactions, and the paucity of these reactions currently limit the chemical features of resulting barcoded products. The present work introduces strain-promoted cycloadditions of cyclic allenes under mild conditions to DNA-encoded library synthesis. Owing to distinct cycloaddition modes of these reactive intermediates with activated olefins, 1,3-dipoles and dienes, the process generates diverse molecular architectures from a single precursor. The resulting DNA-barcoded compounds exhibit unprecedented ring and topographic features—related to elements found to be powerful in phenotypic screening." @default.
- W4236501171 created "2022-05-12" @default.
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- W4236501171 date "2019-12-17" @default.
- W4236501171 modified "2023-10-16" @default.
- W4236501171 title "Water-Compatible Cycloadditions of Oligonucleotide-Conjugated Strained Allenes for DNA-Encoded Library Synthesis" @default.
- W4236501171 doi "https://doi.org/10.26434/chemrxiv.11342471" @default.
- W4236501171 hasPublicationYear "2019" @default.
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